Abstract
Purpose
To evaluate the short-term efficacy of intravitreal triamcinolone (IVTA) injection for the treatment of macular edema secondary to branch retinal vein occlusion (BRVO) refractory to intravitreal bevacizumab injections.
Methods
This retrospective, observational study included 23 eyes of 23 patients with macular edema secondary to BRVO. The patients with macular edema unresponsive to 2 or more consecutive monthly intravitreal bevacizumab injections were treated with IVTA. Best-corrected visual acuity (BCVA) and central foveal thickness (CFT) based on optical coherence tomography were evaluated before IVTA and 1 month and 3 months after IVTA injections.
Results
All patients were previously treated with 3.4 ± 1.2 intravitreal bevacizumab injections. The IVTA injection was performed at 4.3 ± 1.7 weeks after the last bevacizumab injection. The logarithm of the minimal angle of resolution (log MAR) BCVA was also decreased from 0.61 ± 0.45 to 0.52 ± 0.35 after 1 month and to 0.58 ± 0.37 after 3 months of IVTA, although without statistical significance (p = 0.114 and 0.412, respectively). Eight eyes (34.8%) showed more than 3 lines improvement of BCVA and 4 eyes (17.4%) showed stable BCVA increasing 2 lines or less. CFT was significantly improved from 512 ± 166 μ m to 310 ± 139 μ m after 1 month and to 324 ± 159 μ m after 3 months of IVTA injections (p = 0.014 and 0.031, respectively).
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Table 1.
Data | |
---|---|
Age (years) | 58.6 ± 8.4 (41–78) |
Gender (n, %) | |
Male | 10 (43.5) |
Female | 13 (56.5) |
Classification (n, %) | |
Non-ischemic type | 16 (69.6) |
Ischemic type | 7 (30.4) |
Baseline BCVA (log MAR) | 0.65 ± 0.41 |
(range CF-20/30) | |
Mean baseline CFT (μ m)* | 562 ± 156 |
(range 322–798) | |
BCVA (log MAR) before IVTA | 0.61 ± 0.45 |
(range CF-20/30) | |
Mean baseline CFT (μ m) before IVTA† | 512 ± 166 |
(range 302–772) | |
Number of bevacizumab injections | 3.4 ± 1.2 (3–5) |
before IVTA | |
Lens status (n, %) | |
Phakia | 17 (73.9) |
Pseudophakia | 6 (26.1) |
Macular edema type (n, %) | |
Combined with SRD | 12 (52.2) |
Without SRD component | 11 (47.8) |
Values are presented as mean ± SD (range) or n (%) unless other-wise indicated. BCVA = best corrected visual acuity; log MAR = logarithm of the minimum angle of resolution; CF = counting finger; CFT = central foveal thickness; IVTA = intravitreal triamcinolone injection; SRD = sensory retinal detachment; SD = standard deviation.
Table 2.
Response group (n = 12) | Non-response group (n = 1 | 1) p-value | |
---|---|---|---|
Age | 61.6 ± 8.1 | 57.3 ± 6.4 | 0.672* |
Classification (n, %) | |||
Perfused type | 9 (75.0) | 7 (63.6) | 0.554† |
Ischemic type | 3 (25.0) | 4 (36.4) | |
Lens status (n, %) | |||
Phakia | 8 (66.7) | 7 (63.6) | 0.882† |
Pseudophakia | 4 (33.3) | 4 (36.4) | |
Baseline BCVA (log MAR) (Snellen equivalent) | 0.60 ± 0.49 | 0.63 ± 0.33 | 0.672* |
Baseline central macular thickness (μ m) | 498 ± 191 | 533 ± 186 | 0.125* |
Time from baseline to triamcinolone injection (months) | 4.2 ± 1.2 | 4.4 ± 1.8 | 0.912* |
Macular edema type | |||
With SRD | 8 | 4 | 0.115† |
Without SRD | 4 | 7 |